Medical visits of childhood cancer survivors in Japan: A cross‐sectional survey |
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Authors: | Shuichi Ozono Naoko Maeda Jun Okamura Keiko Asami Tsuyako Iwai Kiyoko Kamibeppu Naoko Sakamoto Naoko Kakee Keizo Horibe |
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Affiliation: | 1. Department of Pediatrics, Kurume University School of Medicine;2. Department of Pediatrics and Clinical Research Center, Nagoya Medical Center, Aichi;3. Institute for Clinical Research, National Kyusyu Cancer Center, Fukuoka;4. Department of Pediatrics, Niigata Cancer Center Hospital, Niigata;5. Department of Hemato‐oncology, Kagawa Children's Hospital, Kagawa, Japan;6. Department of Family Nursing, The University of Tokyo, and Departments of;7. Epidemiology;8. Health Policy, National Research Institute for Child Health and Development, Tokyo |
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Abstract: | Background: Although more children with cancer continue to be cured, these survivors experience various late effects. Details of the medical visit behaviors of childhood cancer survivors (CCS) in adulthood remain to be elucidated. Methods: In order to examine medical visits in the past and future of CCS, we performed a cross‐sectional survey with self‐rating questionnaires on medical visits of CCS compared with control groups (their siblings and the general population). Results: Questionnaires were completed by 185 CCS, 72 of their siblings and 1000 subjects from the general population and the results were analyzed. Mean ages at this survey and the duration after therapy completions of CCS were 23 and 12 years, respectively. We found that the previous treatment hospitals (where CCS were treated for their cancer) were the most commonly visited medical facilities for the CCS group (74% for female patients and 64% for male patients) and more than half of the CCS preferred to continue visiting the previous treatment hospital with enough satisfaction in Japan. The multivariate analysis showed that female sex and relapse were significantly associated with the past visits to the previous treatment hospital and that the CCS with brain tumors or bone/soft tissue sarcomas and CCS with any late effects tended to continue the relationships with the hospital. In addition female sex was also significantly associated with desired future visits to the previous treatment hospital. On the other hand, the married CCS tended to be disinclined to visit the hospital it in the future. Conclusions: In order to optimize risk‐based care and promote health for CCS after adulthood, we should discuss the medical transition with CCS and their parents. |
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Keywords: | childhood cancer survivors cross‐sectional survey health care medical visit transition |
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